Canonical Allele Identifier: CA428305762

Gene: IL1RN

Linked Data

• MyVariant Identifiers: chr2:g.113875601T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118024T>G , CM000664.2:g.113118024T>G	GRCh38
NC_000002.11:g.113875601T>G , CM000664.1:g.113875601T>G	GRCh37
NC_000002.10:g.113592072T>G	NCBI36
NG_021240.1:g.5132T>G , LRG_188:g.5132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2042T>G	ENSP00000387210.1:n.-272-2042T>G
ENST00000465812.6:n.775+359T>G
ENST00000696881.1:c.-277T>G	ENSP00000512949.1:n.-277T>G
ENST00000259206.9:c.6T>G	ENSP00000259206.5:p.Ala2=
ENST00000354115.6:c.6T>G	ENSP00000329072.3:p.Ala2=
ENST00000361779.7:c.-214T>G	ENSP00000354816.3:n.-214T>G
ENST00000409052.5:c.-272-2042T>G	ENSP00000387210.1:n.-272-2042T>G
ENST00000486167.1:n.44T>G
NM_000577.4:c.6T>G	NP_000568.1:p.Ala2=
NM_173841.2:c.6T>G , LRG_188t1:c.6T>G	NP_776213.1:p.Ala2=
NM_173843.2:c.-214T>G	NP_776215.1:n.-214T>G
XM_006712497.2:c.-277T>G	XP_006712560.1:n.-277T>G
XM_011511121.1:c.-272-2042T>G	XP_011509423.1:n.-272-2042T>G
NM_001318914.1:c.-277T>G	NP_001305843.1:n.-277T>G
NM_000577.5:c.6T>G	NP_000568.1:p.Ala2=
NM_001318914.2:c.-277T>G	NP_001305843.1:n.-277T>G
NM_173843.3:c.-214T>G	NP_776215.1:n.-214T>G
NM_173841.3:c.6T>G	NP_776213.1:p.Ala2=